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I Denjoy

Showing results (71-80 of 78) with videos related to

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European Heart Journal|March 21, 1998
Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndromeN Neyroud, P Maison-Blanche, I Denjoy, et al.
Circulation Research|February 19, 1999
Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndromeN Neyroud, P Richard, N Vignier, et al.
Circulation|February 27, 2001
Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutationsJ M Lupoglazoff, I Denjoy, M Berthet, et al.
Circulation|March 23, 1999
C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrenceM Berthet, I Denjoy, C Donger, et al.
Journal of Medical Genetics|November 8, 2005
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patientsA V Postma, I Denjoy, J Kamblock, et al.
Circulation|September 8, 1999
Splicing mutations in KCNQ1: a mutation hot spot at codon 344 that produces in frame transcriptsA Murray, C Donger, C Fenske, et al.
Scientific Reports|August 31, 2018
High prevalence of ventricular repolarization abnormalities in people carrying TGFβR2 mutationsF Extramiana, O Milleron, S Elbitar, et al.
Circulation|January 4, 2001
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmiasP J Schwartz, S G Priori, C Spazzolini, et al.
Pageof 8

Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
European Heart Journal|March 21, 1998
Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndromeN Neyroud, P Maison-Blanche, I Denjoy, et al.
Circulation Research|February 19, 1999
Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndromeN Neyroud, P Richard, N Vignier, et al.
Circulation|February 27, 2001
Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutationsJ M Lupoglazoff, I Denjoy, M Berthet, et al.
Circulation|March 23, 1999
C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrenceM Berthet, I Denjoy, C Donger, et al.
Journal of Medical Genetics|November 8, 2005
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patientsA V Postma, I Denjoy, J Kamblock, et al.
Circulation|September 8, 1999
Splicing mutations in KCNQ1: a mutation hot spot at codon 344 that produces in frame transcriptsA Murray, C Donger, C Fenske, et al.
Scientific Reports|August 31, 2018
High prevalence of ventricular repolarization abnormalities in people carrying TGFβR2 mutationsF Extramiana, O Milleron, S Elbitar, et al.
Circulation|January 4, 2001
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmiasP J Schwartz, S G Priori, C Spazzolini, et al.
Pageof 8